Martinelli, Ilenia, Di Bonaventura, Maria Vittoria Micioni, Moruzzi, Michele, Amantini, Consuelo, Maggi, Federica, Gabrielli, Maria Gabriella, Fruganti, Alessandro, Marchegiani, Andrea, Dini, Fabrizio, Marini, Carlotta, Polidori, Carlo, Lupidi, Giulio, Amenta, Francesco, Tayebati, Seyed Khosrow, Cifani, Carlo, Tomassoni, Daniele, Martinelli, Ilenia, Di Bonaventura, Maria Vittoria Micioni, Moruzzi, Michele, Amantini, Consuelo, Maggi, Federica, Gabrielli, Maria Gabriella, Fruganti, Alessandro, Marchegiani, Andrea, Dini, Fabrizio, Marini, Carlotta, Polidori, Carlo, Lupidi, Giulio, Amenta, Francesco, Tayebati, Seyed Khosrow, Cifani, Carlo, and Tomassoni, Daniele
The accumulation of adipose tissue increases the risk of several diseases. The fruits-intake, containing phytochemicals, is inversely correlated with their development. This study evaluated the effects of anthocyanin-rich tart cherries in diet-induced obese (DIO) rats. DIO rats were exposed to a high-fat diet with the supplementation of tart cherry seeds powder (DS) and seed powder plus juice (DJS). After 17 weeks, the DIO rats showed an increase of body weight, glycaemia, insulin, and systolic blood pressure. In the DS and DJS groups, there was a decrease of systolic blood pressure, glycaemia, triglycerides, and thiobarbituric reactive substances in the serum. In the DJS rats, computed tomography revealed a decrease in the spleen-to-liver attenuation ratio. Indeed, sections of the DIO rats presented hepatic injury characterized by steatosis, which was lower in the supplemented groups. In the liver of the DIO compared with rats fed with a standard diet (CHOW), a down-regulation of the GRP94 protein expression and a reduction of LC3- II/LC3-I ratio were found, indicating endoplasmic reticulum stress and impaired autophagy flux. Interestingly, tart cherry supplementation enhanced both unfolded protein response (UPR) and autophagy. This study suggests that tart cherry supplementation, although it did not reduce body weight in the DIO rats, prevented its related risk factors and liver steatosis.